Efficacy of Aldosterone Antagonist Therapy for Prevention of New Atrial Fibrillation
Primary Purpose
AFib
Status
Recruiting
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Spironolactone
No Spironolactone
Sponsored by
About this trial
This is an interventional treatment trial for AFib
Eligibility Criteria
Inclusion Criteria:
- diagnosis of typical AFL confirmed by 12-lead ECG
- no documented AF on ECG, ambulatory monitor, pacemaker or ICD at any time
- scheduled to undergo catheter ablation of the CTI for treatment of AFL
- history of hypertension (HTN) or heart failure (HF) (reduced or preserved systolic function)
Exclusion Criteria:
- history of known AF episodes
- previous CTI or PVI ablation procedure
- other SVT mechanisms demonstrated (AVNRT, AVRT or accessory pathways)
- amiodarone usage within the past 3 months,
- unwillingness to participate or undergo insertable monitor implantation
- hyperkalemia (potassium > 5.0 mEq/L)
- severe renal disease (Cr >2.5 mg/dL [men], >2.0 mg/dL [women, GFR < 30 mL/min/1.73 m2)
- life expectancy < 18 months
- prior intolerance to treatment with an aldosterone antagonist
- current treatment with an aldosterone antagonist
- need for treatment with a class I or III AAD for another indication
- operative AFL (occurring within 30 days of surgery) that is expected to resolve
- presence of a cardiac rhythm device (pacemaker or ICD) capable of AF monitoring
- currently pregnant or nursing a child
- unwilling not to become pregnant and to use birth control while taking spironolactone
Sites / Locations
- Piedmont Heart InstituteRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Standard Therapy
Interventional Therapy
Arm Description
subjects undergoing CTI ablation
subjects treated with an aldosterone antagonist after CTI ablation
Outcomes
Primary Outcome Measures
Long-Term incidence of new-onset AF after CTI ablation
1. To accurately determine the long-term incidence of new-onset AF after CTI ablation using an implantable rhythm monitor
Rates of new-onset AF between standard therapy and spironolactone
2. To compare the rates of new onset AF in subjects randomized to standard medical therapy following CTI ablation compared with those randomized to treatment with an aldosterone antagonist (spironolactone)
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03929718
Brief Title
Efficacy of Aldosterone Antagonist Therapy for Prevention of New Atrial Fibrillation
Official Title
A Randomized Prospective Pilot Study to Evaluate Efficacy of Aldosterone Antagonist Therapy for Prevention of New Atrial Fibrillation (AF) in Patients With Atrial Flutter (AFL), But no Previously Detected AF, Undergoing caVOtricuspID Isthmus Ablation
Study Type
Interventional
2. Study Status
Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 24, 2019 (Actual)
Primary Completion Date
May 2023 (Anticipated)
Study Completion Date
May 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Piedmont Healthcare
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to accurately determine, using an implantable rhythm monitor, the long-term incidence of new atrial fibrillation after ablation of atrial flutter in those treated with spironolactone compared with standard medical therapy.
Detailed Description
Catheter ablation of the cavotricuspid isthmus (CTI) is an effective and safe procedure in patients with atrial flutter (AFL) with excellent long-term results in preventing AFL recurrences. However, new-onset atrial fibrillation (AF) commonly develops after this procedure and has important clinical implications for patient management. Few studies have assessed the long-term incidence and prevalence of AF after CTI ablation via intensive continuous rhythm monitoring with an implantable cardiac monitor. Furthermore, whether the development of AF can be impacted beneficially by adjunctive therapeutic approaches is not known. The co-primary objectives of this pilot study in patients with typical atrial flutter (AFL) but no previously detected AF are: 1) to accurately determine the long-term incidence of new-onset AF after CTI ablation using an implantable rhythm monitor; 2) to compare the rates of new onset AF in subjects randomized to standard, usual-care, medical therapy following CTI ablation compared with those randomized to treatment with an aldosterone antagonist (spironolactone) in addition to their usual care medications. The patient population will be subjects with typical atrial flutter and a history of hypertension or heart failure, but no known AF episodes, scheduled to undergo catheter ablation of the CTI for treatment of AFL. Patients will be randomized to remain on their standard, usual-care. medications or to take oral spironolactone (a standard, FDA-approved medication used in the treatment of hypertension and heart failure) starting after their ablation procedure. The primary study endpoint will be any atrial tachyarrhythmia episode (AF, AFL or atrial tachycardia) lasting greater than one minute detected via the implanted cardiac monitor after CTI ablation during long-term follow-up. The incidence of new-onset AF after CTI ablation will be compared between subjects randomized to be treated with usual care vs. those treated with usual care plus spironolactone on an intention to treat basis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
AFib
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Model Description
Randomized, pilot study
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Standard Therapy
Arm Type
Active Comparator
Arm Description
subjects undergoing CTI ablation
Arm Title
Interventional Therapy
Arm Type
Experimental
Arm Description
subjects treated with an aldosterone antagonist after CTI ablation
Intervention Type
Drug
Intervention Name(s)
Spironolactone
Intervention Description
receive spironolactone treatment after CTI ablation
Intervention Type
Drug
Intervention Name(s)
No Spironolactone
Intervention Description
no spironolactone treatment
Primary Outcome Measure Information:
Title
Long-Term incidence of new-onset AF after CTI ablation
Description
1. To accurately determine the long-term incidence of new-onset AF after CTI ablation using an implantable rhythm monitor
Time Frame
24 months
Title
Rates of new-onset AF between standard therapy and spironolactone
Description
2. To compare the rates of new onset AF in subjects randomized to standard medical therapy following CTI ablation compared with those randomized to treatment with an aldosterone antagonist (spironolactone)
Time Frame
24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
diagnosis of typical AFL confirmed by 12-lead ECG
no documented AF on ECG, ambulatory monitor, pacemaker or ICD at any time
scheduled to undergo catheter ablation of the CTI for treatment of AFL
history of hypertension (HTN) or heart failure (HF) (reduced or preserved systolic function)
Exclusion Criteria:
history of known AF episodes
previous CTI or PVI ablation procedure
other SVT mechanisms demonstrated (AVNRT, AVRT or accessory pathways)
amiodarone usage within the past 3 months,
unwillingness to participate or undergo insertable monitor implantation
hyperkalemia (potassium > 5.0 mEq/L)
severe renal disease (Cr >2.5 mg/dL [men], >2.0 mg/dL [women, GFR < 30 mL/min/1.73 m2)
life expectancy < 18 months
prior intolerance to treatment with an aldosterone antagonist
current treatment with an aldosterone antagonist
need for treatment with a class I or III AAD for another indication
operative AFL (occurring within 30 days of surgery) that is expected to resolve
presence of a cardiac rhythm device (pacemaker or ICD) capable of AF monitoring
currently pregnant or nursing a child
unwilling not to become pregnant and to use birth control while taking spironolactone
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bola Ajose
Phone
404-605-2875
Email
Bola.Ajose@piedmont.org
First Name & Middle Initial & Last Name or Official Title & Degree
Julia Daugherty
Phone
404-605-2301
Email
Julia.Daugherty@piedmont.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bruce Stambler, MD
Organizational Affiliation
Piedmont Healthcare
Official's Role
Principal Investigator
Facility Information:
Facility Name
Piedmont Heart Institute
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30309
Country
United States
Individual Site Status
Recruiting
12. IPD Sharing Statement
Learn more about this trial
Efficacy of Aldosterone Antagonist Therapy for Prevention of New Atrial Fibrillation
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